1. Acids and Bases Functional Groups Polarity Intermolecular Forces Acids and Bases Functional Groups

3. Electronegativity Trends Ability to Attract the Electrons in a Covalent Bond

6. © 2013 Pearson Education, Inc. Dipole Moment Dipole moment is defined to be the amount of charge separation (  ) multiplied by the bond length (  ). Charge separation is shown by an electrostatic potential map (EPM), where red indicates a partially negative region and blue indicates a partially positive region. Chapter 16

7. Methanol

8. Dipole Moment (  ) is sum of the Bond Moments

9. © 2013 Pearson Education, Inc. Molecular Dipole Moment The molecular dipole moment is the vector sum of the bond dipole moments. Depends on bond polarity and bond angles. Lone pairs of electrons contribute significantly to the dipole moment. Chapter 29

10. Nonpolar Compounds Bond Moments Cancel Out

11. A Model of a Saturated Hydrocarbon

12. Lone Pairs and Dipole Moments Chapter 212

13. Nitromethane

14. Dipole Moment reflects Both Resonance Structures

15. Intermolecular Forces Strength of attractions between molecules influences the melting point (m. p.), boiling point (b. p.), and solubility of compounds. Classification of attractive forces: – Dipole–dipole forces – London dispersions forces – Hydrogen bonding in molecules with —OH or — NH groups Chapter 215

16. Dipole–Dipole Interaction Chapter 216

17. London Dispersions Chapter 217

18. © 2013 Pearson Education, Inc. Effect of Branching on Boiling Point The long-chain isomer (n-pentane) has the greatest surface area and therefore the highest boiling point. As the amount of chain branching increases, the molecule becomes more spherical and its surface area decreases. The most highly branched isomer (neopentane) has the smallest surface area and the lowest boiling point. Chapter 218

20. Hydrogen Bonds Chapter 220

22. Rank the following compounds in order of increasing boiling points. Explain the reasons for your chosen order. Solved Problem 4 Chapter 222

23. To predict relative boiling points, we should look for differences in (1) hydrogen bonding, (2) molecular weight and surface area, and (3) dipole moments. Except for neopentane, these compounds have similar molecular weights. Neopentane is the lightest, and it is a compact spherical structure that minimizes van der Waals attractions. Neopentane is the lowest-boiling compound. Neither n-hexane nor 2,3-dimethylbutane is hydrogen bonded, so they will be next higher in boiling points. Because 2,3-dimethylbutane is more highly branched (and has a smaller surface area) than n-hexane, 2,3-dimethylbutane will have a lower boiling point than n-hexane. Solution The two remaining compounds are both hydrogen bonded, and pentan-1-ol has more area for van der Waals forces. Therefore, pentan-1-ol should be the highest-boiling compound. We predict the following order: neopentane < 2,3-dimethylbutane < n-hexane < 2-methylbutan-2-ol < pentan-1-ol The actual boiling points are given here to show that our prediction is correct. 10 °C58 °C69 °C102 °C138 °C Chapter 223

24. Polarity Effects on Solubility Like dissolves like. Polar solutes dissolve in polar solvents. Nonpolar solutes dissolve in nonpolar solvents. Molecules with similar intermolecular forces will mix freely. Chapter 224

28. Definitions of Acids/Bases

29. Dissociation in H 2 O Arrhenius Acid forms H 3 O + Bronsted-Lowry Acid donates a H +

30. Brønsted-Lowry Acids and Bases Brønsted-Lowry acids are any species that donate a proton. Brønsted-Lowry bases are any species that can accept a proton. Chapter 130

31. © 2013 Pearson Education, Inc. Conjugate Acids and Bases Conjugate acid: when a base accepts a proton, it becomes an acid capable of returning that proton. Conjugate base: when an acid donates its proton, it becomes capable of accepting that proton back. Chapter 131

32. Acid Strength defined by pK a

34. Stronger Acid Controls Equilibrium

35. Reaction Described with Arrows

36. Equilibrium Reactions

39. Identify the Acid and Base

40. Equilibrium Favors Reactants

41. The Effect of Resonance on pKa

42. Effect of Electronegativity on pK a As the bond to H becomes more polarized, H becomes more positive and the bond is easier to break. Chapter 142

44. Effect of Size on pK a As size increases, the H is more loosely held and the bond is easier to break. A larger size also stabilizes the anion. Chapter 144

47. Lewis Acids and Lewis Bases Lewis bases are species with available electrons than can be donated to form a new bond. Lewis acids are species that can accept these electrons to form new bonds. Since a Lewis acid accepts a pair of electrons, it is called an electrophile. Chapter 147

48. Nucleophiles and Electrophiles Nucleophile: Donates electrons to a nucleus with an empty orbital (same as Lewis Base) Electrophile: Accepts a pair of electrons (same as Lewis Acid) When forming a bond, the nucleophile attacks the electrophile, so the arrow goes from negative to positive. When breaking a bond, the more electronegative atom receives the electrons. Chapter 148

49. Nucleophiles and Electrophiles Chapter 149